Literature DB >> 18788877

Anatomical basis for apparent subepithelial cleft lip: a histological and ultrasonographic survey of the orbicularis oris muscle.

Carolyn R Rogers1, Seth M Weinberg, Timothy D Smith, Frederic W B Deleyiannis, Mark P Mooney, Mary L Marazita.   

Abstract

OBJECTIVE: To determine if there is an anatomic basis for subepithelial orbicularis oris muscle defects by directly comparing ultrasonographic images of the upper lip with corresponding histological sections obtained from cadavers.
METHODS: Ultrasound was performed on the upper lips of previously frozen, unpreserved cadaver heads (n = 32), followed by dissection and sectioning of the upper lips. The ultrasound sequences were scored by a panel of raters, classifying the orbicularis oris muscle as negative, positive, or unknown for the presence of an orbicularis oris discontinuity (subepithelial defect). Based on ultrasound, six lip specimens were chosen for histological sectioning, were stained with hematoxylin-eosin and Gomori trichrome stain, and were evaluated with light microscopy at low (8x) and intermediate (100x) magnification.
RESULTS: One cadaver was scored positive for an orbicularis oris muscle discontinuity based on ultrasound; whereas, the remaining cadavers were scored negative. Of the cadavers with negative ultrasound scores, two were noted to have orbicularis oris muscles with "irregular" features (e.g., excessive localized thinning or asymmetry). From histology, the area of discontinuity as visualized on the positively scored ultrasound was characterized by both disorganized orbicularis oris muscle fibers and excess connective tissue within the muscle belly. In contrast, the localized thinning observed on some of the negatively scored ultrasounds was not confirmed by histology.
CONCLUSIONS: Abnormalities of the orbicularis oris muscle visualized by ultrasound have an anatomic basis as revealed through histology. Ultrasound is a useful tool for noninvasively identifying discontinuities of the orbicularis oris muscle.

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Year:  2007        PMID: 18788877     DOI: 10.1597/07-115.1

Source DB:  PubMed          Journal:  Cleft Palate Craniofac J        ISSN: 1055-6656


  13 in total

1.  Nasolabial fold discontinuity during speech as a possible extended cleft phenotype.

Authors:  Karen L Schmidt; Katherine Neiswanger; Ellen Cohn; Rebecca Desensi; Carla Brandon; Kathleen Bardi; Mary L Marazita
Journal:  Cleft Palate Craniofac J       Date:  2012-01-24

Review 2.  Folic acid and orofacial clefts: a review of the evidence.

Authors:  G L Wehby; J C Murray
Journal:  Oral Dis       Date:  2010-01       Impact factor: 3.511

Review 3.  Genetics of cleft lip and cleft palate.

Authors:  Elizabeth J Leslie; Mary L Marazita
Journal:  Am J Med Genet C Semin Med Genet       Date:  2013-10-04       Impact factor: 3.908

Review 4.  Cleft lip and palate: understanding genetic and environmental influences.

Authors:  Michael J Dixon; Mary L Marazita; Terri H Beaty; Jeffrey C Murray
Journal:  Nat Rev Genet       Date:  2011-03       Impact factor: 53.242

5.  [Comparative ultrasonographic and histomorphologic examination of the lips].

Authors:  F L Lefarth; A Prescher; W Angerstein
Journal:  HNO       Date:  2014-12       Impact factor: 1.284

6.  Application of ultrasound imaging of upper lip orbicularis oris muscle.

Authors:  Wen-Hao Zhang; Yuan-Yuan Chen; Jun-Jie Liu; Xin-Hong Liao; Yang-Chun Du; Yong Gao
Journal:  Int J Clin Exp Med       Date:  2015-03-15

Review 7.  The evolution of human genetic studies of cleft lip and cleft palate.

Authors:  Mary L Marazita
Journal:  Annu Rev Genomics Hum Genet       Date:  2012-06-06       Impact factor: 8.929

8.  Revisiting the recurrence risk of nonsyndromic cleft lip with or without cleft palate.

Authors:  Cherise M Klotz; Xiaojing Wang; Rebecca S Desensi; Robin E Grubs; Bernard J Costello; Mary L Marazita
Journal:  Am J Med Genet A       Date:  2010-11       Impact factor: 2.802

9.  Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.

Authors:  Satoshi Suzuki; Mary L Marazita; Margaret E Cooper; Nobutomo Miwa; Anne Hing; Astanand Jugessur; Nagato Natsume; Kazuo Shimozato; Naofumi Ohbayashi; Yasushi Suzuki; Teruyuki Niimi; Katsuhiro Minami; Masahiko Yamamoto; Tserendorj J Altannamar; Tudevdorj Erkhembaatar; Hiroo Furukawa; Sandra Daack-Hirsch; Jamie L'heureux; Carla A Brandon; Seth M Weinberg; Katherine Neiswanger; Frederic W B Deleyiannis; Javier E de Salamanca; Alexandre R Vieira; Andrew C Lidral; James F Martin; Jeffrey C Murray
Journal:  Am J Hum Genet       Date:  2009-02-26       Impact factor: 11.025

10.  Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes.

Authors:  Elizabeth J Leslie; Jennifer L Mancuso; Brian C Schutte; Margaret E Cooper; Kate M Durda; Jamie L'Heureux; Theresa M Zucchero; Mary L Marazita; Jeffrey C Murray
Journal:  Am J Med Genet A       Date:  2013-08-15       Impact factor: 2.802

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